777 results
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31ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Crosstex VH2O2 Chemical Indicators
FDA 510(k)
FDA Class 2
·General Hospital
Darby Dental Supply, LLC
FDA UDI
DARBY DENTAL SUPPLY, LLC·00889813028377·MOUTH PROP TAN SILICONE L DARBY
Zirlux
FDA UDI
HENRY SCHEIN, INC.·00304040187975·ZIRLUX ML DISC OM2 98x22
cut guide, fulcrum, seeker
FDA UDI
Treace Medical Concepts, Inc.·00810111221658·Mini 3 in 1 Left
DEBAKEY NEEDLE PULLING FORCEPS
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896059641·DEBAKEY NEEDLE PULLING TISSUE FORCEPS TUNGSTEN ...
Initia Total Hip System
FDA UDI
KYOCERA CORPORATION·04547898307171·STDHO LINER 28-44
ESTHETIC EASE ABUTMENTS FOR THE ITI DENTAL IMPLANT SYSTEM
FDA 510(k)
FDA Class 2
·Dental
ONTRAK TESTSTIK FOR METHAMPHETAMINE, CAT. 1986686
FDA 510(k)
FDA Class 2
·Clinical Toxicology
BD VACUTAINER® K2 EDTA (K2E) 5.4MG BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·June 21, 2023
ANALYTICAL E MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·October 15, 2008
COBAS 6000 C501 MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code CEM·August 10, 2011
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·July 1, 2013
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·November 8, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·July 28, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 11, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 4, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 11, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 21, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·October 25, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·July 24, 2021